• Journal of Korean Society of Industrial and Systems Engineering
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• v.19 no.39
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• pp.27-36
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• 1996

The objective of this paper is to outline an integrated cellular manufacturing system (ICMS) which integrates process planning and scheduling in the cellular manufacturing environment. It combines design systems with manufacturing systems in batch production. Furthermore, it is developed to overcome the difficulties that exist in the current manufacturing practices.

• The Journal of Korean Institute of Electromagnetic Engineering and Science
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• v.12 no.7
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• pp.1037-1047
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• 2001

In this paper, the capacity for the reverse link of the imperfect power controlled DS/CDMA hierarchical cellular system is analyzed considering imperfect sectorization in shadowing environment. Unlike the theoretical assumption, the power control of the DS/CDMA hierarchical cellular system is not perfect. Therefore, we consider various parameters such as the imperfect power control, the imperfect sectorization, the processing gain and the number of microcell interferers, which cause the capacity variation of the DS/CDMA hierarchical cellular system. It is shown that the capacity of DS/CDMA hierarchical cellular system is decreased according to the increase of the deviation of the imperfect power control, the overlapped angle, the power ratio between macrocell and microcell and to the decrease of processing gain, the number of microcell interfering users. Also, it is observed that the hierarchical cellular system can increase the user capacity from 1.54 to 3.89 times compared to the homogeneous macro-cellular system.

• Microbiology and Biotechnology Letters
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• v.49 no.4
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• pp.478-484
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• 2021

Cellular resources including transcriptional and translational machineries in bacteria are limited, yet microorganisms depend upon them to maximize cellular fitness. Bacteria have evolved strategies for using resources economically. Regulatory networks for the gene expression system enable the cell to synthesize proteins only when necessary. At the same time, regulatory interactions enable the cell to limit losses when the system cannot make a cellular profit due to fake substrates. Also, the architecture of the gene expression flow can be advantageous for clustering functionally related products, thus resulting in effective interactions among molecules. In addition, cellular systems modulate the investment of proteomes, depending upon nutrient qualities, and fast-growing cells spend more resources on the synthesis of ribosomes, whereas nonribosomal proteins are synthesized in nutrient-limited conditions. A deeper understanding of cellular mechanisms underlying the optimal allocation of cellular resources can be used for biotechnological purposes, such as designing complex genetic circuits and constructing microbial cell factories.

• Proceedings of the Korea Concrete Institute Conference
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• 1999.04a
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• pp.825-830
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• 1999

The purpose of this study is to improve overall performance of prefoamed lightweight cellular concrete for On-Dol system floor. This study includes 4 sections as follows. \circled1 Analysis of the structural characteristics of On-Dol System focusing on the lightweight cellular concrete insulation layer. \circled2 Establishment of the mixing design equations. \circled3 Development of some admixtures used with foaming agent. \circled4 Improvement of the equipment for onsite production. This study has proven that, compared with the current existing one, the newly developed lightweight cellular concrete has been reduced the usage of cement by 20% and the cracks caused by cement drying shrinkage up to 80% but has shown the increased compression strength by 20% at 7 days curing period. The volume contraction of freshly prepared cellular concrete by the loss of foam was hardly found in newly developed lightweight cellular concrete.

• Molecules and Cells
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• v.27 no.3
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• pp.337-343
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• 2009

We developed a novel on-chip activity assay using protein arrays for quantitative and rapid analysis of transglutaminase activity in mammalian cells. Transglutaminases are a family of $Ca^{2+}$-dependent enzymes involved in cell regulation as well as human diseases such as neurodegenerative disorders, inflammatory diseases and tumor progression. We fabricated the protein arrays by immobilizing N,N'-dimethylcasein (a substrate) on the amine surface of the arrays. We initiated transamidating reaction on the protein arrays and determined the transglutaminase activity by analyzing the fluorescence intensity of biotinylated casein. The on-chip transglutaminase activity assay was proved to be much more sensitive than the $[^3H]putrescine$-incorporation assay. We successfully applied the on-chip assay to a rapid and quantitative analysis of the transglutaminase activity in all-trans retinoic acid-treated NIH 3T3 and SH-SY5Y cells. In addition, the on-chip transglutaminase activity assay was sufficiently sensitive to determine the transglutaminase activity in eleven mammalian cell lines. Thus, this novel on-chip transglutaminase activity assay was confirmed to be a sensitive and high-throughput approach to investigating the roles of transglutaminase in cellular signaling, and, moreover, it is likely to have a strong potential for monitoring human diseases.

• The Journal of Korean Institute of Communications and Information Sciences
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• v.25 no.4A
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• pp.481-488
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• 2000

The demands for mobile communication service are growing rapidly. In heavily populated areas, cell split is unavoidable to increase the capacity of the cellular system. Cell splitting makes a cellular system to have mixed cell sizes. For cell planning, it is necessary to analyze the reverse link capacity of a CDMA cellular system with mixed cell sizes. In this paper, we propose a method to calculate the reverse link capacity of a CDMA cellular system with mixed cell sizes. When a macro cell is split into three micro cells, as an example, we calculate the reverse link capacities for the three micro cells and the neighboring macro cells. The results show that as the radius of a micro cell decreases, the reverse link capacity of the micro cell increases, while those of the neighboring macro cells decrease.

• Microbiology and Biotechnology Letters
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• v.23 no.5
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• pp.513-518
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• 1995

To evaluate bile salt-tolerance of lactic acid bacteria (LAB, Lactobacillus acidophilus ATCC 4356, Lactobacillus casei IFO 3533, Streptococcus thermnophilus KCTC 2185, Lactobacillus lactis ATCC 4797, and Lactobacillus bulgaricus ATCC 11842), We investigated the survivals, acid production and $\beta $-galactosidase activity of LAB under anaerobic broth system. Cellular permeability of LAB and their cellular retention of $\beta $-galactosidase were also examined in the same system. Although the growth of LAB was slightly suppressed by 0.3% bile salt, they showed normal growth curve. Streptococcus thermophilus KCTC 2185 was significantly more resistant to bile salt than the others. The $\beta $-galactosidase activity from Streptococcus thermophilus KCTC 2185 and Lactobacillus bulgaricus ATCC 11842 and their cellular retention of $\beta $-galactosidase decreased by 0.3% bile salt. The cellular permeability of LAB in the presence of bile salt increased significantly.

• Journal of the Korean Institute of Telematics and Electronics S
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• v.35S no.3
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• pp.39-46
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• 1998

In the FDMA and TDMA Cellular Systems, call blocking rise when frewquence slots andtime slots are used to ther users. Otherwise, in the CDMA cellular systems, call locking arises when interference level is above 10dB according to call of other users. System capacity is defined to be Erlang capacity that is the number of users when CDMA blocking probability is 1% or 2%. Users number corresponded channel number of AMPS and TDMA cellular systems. In this paper, we proposed new reuse-fraction using square of interference poser and obtained Erlang capacity for reverse link of CDMA cellular system with bit rate $R_{b}$, 9.6kbps and 14.4kbps. As a results, Erlange capacity of CDMA system have more 20.7 and 5.5 times than AMPS and TDMA system and have more form 1 to 4 Erlang thatn Viterbi and Padovani obtaned.d.

• 제어로봇시스템학회:학술대회논문집
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• 2003.10a
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• pp.2451-2456
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• 2003

In biological cell manipulation, manual thrust or penetration of an injection pipette into an egg is currently performed by a skilled operator, relying only on visual feedback information. Massive load of various micro injection of either genes, fluid or cells in the postgenomic era calls a more reliable and automatic micro injection system that can test hundreds of genes or cell types at a single experiment. We initiated to study cellular force sensing in zebrafish eggs as the first step for the development of a more controllable micro injection system by any inexperienced operator. Zebrafish eggs at different developmental stages were collected and an integrated biomanipulation system was employed to measure cellular force during penetrating the egg envelope, the chorion. First of all, the biomanipulation system integrated with cellular force sensing instrument is implemented to measure the penetration force of cell membranes and characterize mechanical properties of zebrafish embryo cells. Furthermore, implementation of cellular force sensing system and calibration are presented. Finally, the cellular force sensing of penetrating cell membranes at each developmental stages was experimentally performed. The results demonstrated that the biomanipulation system with force sensing capability can measure cellular force at real-time while the injection operation is undergoing. The magnitude of the measured force was in the range of several hundreds of uN. The precise real-time measurement should provide the first step forwards for the development of an automatic and reliable injection system of various materials into biological cells.

• The Journal of Korean Institute of Communications and Information Sciences
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• v.33 no.8A
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• pp.829-837
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• 2008

A cellular system with fixed relays is considered to be a technology that can support high data transmission service to wide areas. However, either inter-cell interference or inter-sector interference that can be produced by adding relays to the cellular system with fixed relays does not guarantee high link performance to deteriorate function, so that resource allocation for avoidance of interference is very much important. In the paper, the cellular system performance with repeater relay has been compared with the cellular system performance with relay, and cell coverage expansion at the use of relay repeater has been compared. To compare, this paper has suggested resource allocation method to avoid inter-cell interference and inter-sector interference at installation of fixed relay on the cellular system. The proposed method can allocate different frequency resources on adjacent base stations and relays to reduce interference and to expand high data transmission area, and all of frequency bands are used at each sector to elevate efficiency of the frequency when base stations and relays operate simultaneously.